Canonical Allele Identifier: PA2826369660
Gene: C19orf12 HGNC NCBI

Linked Data

ClinVar Variation Id: 1299224
ClinVar RCV Id: RCV001725849 RCV002539775
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001242975.1:p.Asn90Asp
CA405143017
NM_001256046.3:c.268A>G